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Alan K Percy

Showing results (91-100 of 107) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 12, 2018
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2Jeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
Annals of Neurology|January 22, 2021
Multisite Study of Evoked Potentials in Rett SyndromeJoni N Saby, Timothy A Benke, Sarika U Peters, et al.
American Journal on Intellectual and Developmental Disabilities|November 19, 2020
A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical TrialsMelissa Raspa, Carla M Bann, Angela Gwaltney, et al.
Clinical Genetics|February 22, 2019
Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndromeSarika U Peters, Cary Fu, Bernhard Suter, et al.
Med (New York, N.Y.)|March 5, 2025
Results from the phase 2/3 DAFFODIL study of trofinetide in girls aged 2-4 years with Rett syndromeAlan K Percy, Robin Ryther, Eric D Marsh, et al.
Pediatric Neurology|March 25, 2015
Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosisDaniel C Tarquinio, Wei Hou, Jeffrey L Neul, et al.
Neurology|May 5, 2019
Hand stereotypies: Lessons from the Rett Syndrome Natural History StudyJennifer L Stallworth, Marisela E Dy, Caroline B Buchanan, et al.
Brain Communications|August 17, 2022
Electrophysiological biomarkers of brain function in CDKL5 deficiency disorderJoni N Saby, Patrick J Mulcahey, Alexis E Zavez, et al.
Orphanet Journal of Rare Diseases|August 13, 2024
Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver surveyWalter E Kaufmann, Alan K Percy, Jeffrey L Neul, et al.
Molecular Genetics & Genomic Medicine|March 23, 2022
Analysis of X-inactivation status in a Rett syndrome natural history study cohortXiaolan Fang, Kameryn M Butler, Fatima Abidi, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 12, 2018
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2Jeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
Annals of Neurology|January 22, 2021
Multisite Study of Evoked Potentials in Rett SyndromeJoni N Saby, Timothy A Benke, Sarika U Peters, et al.
American Journal on Intellectual and Developmental Disabilities|November 19, 2020
A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical TrialsMelissa Raspa, Carla M Bann, Angela Gwaltney, et al.
Clinical Genetics|February 22, 2019
Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndromeSarika U Peters, Cary Fu, Bernhard Suter, et al.
Med (New York, N.Y.)|March 5, 2025
Results from the phase 2/3 DAFFODIL study of trofinetide in girls aged 2-4 years with Rett syndromeAlan K Percy, Robin Ryther, Eric D Marsh, et al.
Pediatric Neurology|March 25, 2015
Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosisDaniel C Tarquinio, Wei Hou, Jeffrey L Neul, et al.
Neurology|May 5, 2019
Hand stereotypies: Lessons from the Rett Syndrome Natural History StudyJennifer L Stallworth, Marisela E Dy, Caroline B Buchanan, et al.
Brain Communications|August 17, 2022
Electrophysiological biomarkers of brain function in CDKL5 deficiency disorderJoni N Saby, Patrick J Mulcahey, Alexis E Zavez, et al.
Orphanet Journal of Rare Diseases|August 13, 2024
Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver surveyWalter E Kaufmann, Alan K Percy, Jeffrey L Neul, et al.
Molecular Genetics & Genomic Medicine|March 23, 2022
Analysis of X-inactivation status in a Rett syndrome natural history study cohortXiaolan Fang, Kameryn M Butler, Fatima Abidi, et al.
Pageof 11